Establishing conditions for the storage and elution of rabies virus RNA using FTA registered cards
The Flinders Technology Associates filter paper cards (FTA registered cards) can be used to store nucleic acid from various samples and are easily portable. However, RNA is physicochemically unstable compared with DNA, and appropriate methods have not been established for storage and extraction of R...
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Veröffentlicht in: | Journal of veterinary medical science 2015-01, Vol.77 (4), p.461-461 |
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creator | SAKAI, Takeo ISHII, Ayako SEGAWA, Takao TAKAGI, Yukihiko KOBAYASHI, Yuki ITOU, Takuya |
description | The Flinders Technology Associates filter paper cards (FTA registered cards) can be used to store nucleic acid from various samples and are easily portable. However, RNA is physicochemically unstable compared with DNA, and appropriate methods have not been established for storage and extraction of RNA from FTA registered cards. The present study investigated the optimum conditions for storage and elution of viral RNA (vRNA) using rabies virus (RABV) applied to FTA registered cards. When TE buffer was used, the elution rates of vRNA increased with the length of the elution time. When the cards were stored at -80 degree C or -20 degree C, vRNA was stable over 3 months. Degradation of vRNAs occurred following storage at 4 degree C and room temperature, suggesting that RNA should be extracted from cards as soon as possible if no freezer is available. When we tried to amplify vRNA from RABV-infected animal brains applied to FTA registered cards and stored at -80 degree C for 6 months, we did not detect any amplified products with the primer set for 964 bp of RABV N gene. However, we were able to detect amplified products by increasing the elution time of vRNA from FTA registered cards from 30 min to 24 hr or by changing the primer sets to amplify 290 bp of N gene. Thus, we recommend extending the elution time for damaged or low concentration samples in FTA registered cards. |
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However, RNA is physicochemically unstable compared with DNA, and appropriate methods have not been established for storage and extraction of RNA from FTA registered cards. The present study investigated the optimum conditions for storage and elution of viral RNA (vRNA) using rabies virus (RABV) applied to FTA registered cards. When TE buffer was used, the elution rates of vRNA increased with the length of the elution time. When the cards were stored at -80 degree C or -20 degree C, vRNA was stable over 3 months. Degradation of vRNAs occurred following storage at 4 degree C and room temperature, suggesting that RNA should be extracted from cards as soon as possible if no freezer is available. When we tried to amplify vRNA from RABV-infected animal brains applied to FTA registered cards and stored at -80 degree C for 6 months, we did not detect any amplified products with the primer set for 964 bp of RABV N gene. However, we were able to detect amplified products by increasing the elution time of vRNA from FTA registered cards from 30 min to 24 hr or by changing the primer sets to amplify 290 bp of N gene. Thus, we recommend extending the elution time for damaged or low concentration samples in FTA registered cards.</description><identifier>ISSN: 0916-7250</identifier><identifier>EISSN: 1347-7439</identifier><language>eng</language><subject>Rabies virus</subject><ispartof>Journal of veterinary medical science, 2015-01, Vol.77 (4), p.461-461</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>SAKAI, Takeo</creatorcontrib><creatorcontrib>ISHII, Ayako</creatorcontrib><creatorcontrib>SEGAWA, Takao</creatorcontrib><creatorcontrib>TAKAGI, Yukihiko</creatorcontrib><creatorcontrib>KOBAYASHI, Yuki</creatorcontrib><creatorcontrib>ITOU, Takuya</creatorcontrib><title>Establishing conditions for the storage and elution of rabies virus RNA using FTA registered cards</title><title>Journal of veterinary medical science</title><description>The Flinders Technology Associates filter paper cards (FTA registered cards) can be used to store nucleic acid from various samples and are easily portable. However, RNA is physicochemically unstable compared with DNA, and appropriate methods have not been established for storage and extraction of RNA from FTA registered cards. The present study investigated the optimum conditions for storage and elution of viral RNA (vRNA) using rabies virus (RABV) applied to FTA registered cards. When TE buffer was used, the elution rates of vRNA increased with the length of the elution time. When the cards were stored at -80 degree C or -20 degree C, vRNA was stable over 3 months. Degradation of vRNAs occurred following storage at 4 degree C and room temperature, suggesting that RNA should be extracted from cards as soon as possible if no freezer is available. When we tried to amplify vRNA from RABV-infected animal brains applied to FTA registered cards and stored at -80 degree C for 6 months, we did not detect any amplified products with the primer set for 964 bp of RABV N gene. However, we were able to detect amplified products by increasing the elution time of vRNA from FTA registered cards from 30 min to 24 hr or by changing the primer sets to amplify 290 bp of N gene. 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However, RNA is physicochemically unstable compared with DNA, and appropriate methods have not been established for storage and extraction of RNA from FTA registered cards. The present study investigated the optimum conditions for storage and elution of viral RNA (vRNA) using rabies virus (RABV) applied to FTA registered cards. When TE buffer was used, the elution rates of vRNA increased with the length of the elution time. When the cards were stored at -80 degree C or -20 degree C, vRNA was stable over 3 months. Degradation of vRNAs occurred following storage at 4 degree C and room temperature, suggesting that RNA should be extracted from cards as soon as possible if no freezer is available. When we tried to amplify vRNA from RABV-infected animal brains applied to FTA registered cards and stored at -80 degree C for 6 months, we did not detect any amplified products with the primer set for 964 bp of RABV N gene. However, we were able to detect amplified products by increasing the elution time of vRNA from FTA registered cards from 30 min to 24 hr or by changing the primer sets to amplify 290 bp of N gene. Thus, we recommend extending the elution time for damaged or low concentration samples in FTA registered cards.</abstract></addata></record> |
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source | J-STAGE日本語サイト (Free Access); PubMed Central Open Access; PubMed Central; EZB Electronic Journals Library |
subjects | Rabies virus |
title | Establishing conditions for the storage and elution of rabies virus RNA using FTA registered cards |
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